Evidence map›Paper›PMID 31861757›Full record

ReviewInternational journal of molecular sciences2019

Extracellular Vesicles and Epigenetic Modifications Are Hallmarks of Melanoma Progression.

Francesco Mannavola, Stella D'Oronzo, Mauro Cives, Luigia Stefania Stucci, Girolamo Ranieri, Franco Silvestris, Marco Tucci

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 53 citations in OpenAlex.

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  19. The Role of Exosomes and Their Applications in Cancer.International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Francesco MannavolaDepartment of Biomedical Sciences and Clinical Oncology, University of Bari, 'Aldo Moro', 70121 Bari, Italy.ORCID 0000-0003-2623-4166
Stella D'OronzoDepartment of Biomedical Sciences and Clinical Oncology, University of Bari, 'Aldo Moro', 70121 Bari, Italy.
Mauro CivesDepartment of Biomedical Sciences and Clinical Oncology, University of Bari, 'Aldo Moro', 70121 Bari, Italy.ORCID 0000-0002-3013-1816
Luigia Stefania StucciDepartment of Biomedical Sciences and Clinical Oncology, University of Bari, 'Aldo Moro', 70121 Bari, Italy.
Girolamo RanieriNational Cancer Research Center, Istituto Tumori 'Giovanni Paolo II', 70121 Bari, Italy.
Franco SilvestrisDepartment of Biomedical Sciences and Clinical Oncology, University of Bari, 'Aldo Moro', 70121 Bari, Italy.
Marco TucciDepartment of Biomedical Sciences and Clinical Oncology, University of Bari, 'Aldo Moro', 70121 Bari, Italy.ORCID 0000-0003-4008-4897
University of Bari Aldo Moro · ITIstituto Tumori Bari · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG17536
6 · The paper itself

Abstract

Cutaneous melanoma shows a high metastatic potential based on its ability to overcome the immune system's control. The mechanisms activated for these functions vary extremely and are also represented by the production of a number of extracellular vesicles including exosomes. Other vesicles showing a potential role in the melanoma progression include oncosomes and melanosomes and the majority of them mediate tumor processes including angiogenesis, immune regulation, and modifications of the micro-environment. Moreover, a number of epigenetic modifications have been described in melanoma and abundant production of altered microRNAs (mi-RNAs), non-coding RNAs, histones, and abnormal DNA methylation have been associated with different phases of melanoma progression. In addition, exosomes, miRNAs, and other molecular factors have been used as potential biomarkers reflecting disease evolution while others have been suggested to be potential druggable molecules for therapeutic application.

Indexed as

Epigenesis, GeneticGene Expression Regulation, NeoplasticAnimalsCutaneous Malignant MelanomaDisease ProgressionDNA MethylationExtracellular VesiclesHumansMelanomaMicroRNAsSkin NeoplasmsMicroRNAsepigenetic modificationsextracellular vesiclesmelanomamiRNAs

Identifiers

PMID31861757
PMCPMC6981648
OpenAlexW2995084859

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.